scholarly journals Effects of Diisocyanate Structure and Disulfide Chain Extender on Hard Segmental Packing and Self-Healing Property of Polyurea Elastomers

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 838 ◽  
Author(s):  
Ting Li ◽  
Tianze Zheng ◽  
Jiarui Han ◽  
Zhanli Liu ◽  
Zhao-Xia Guo ◽  
...  

Four linear polyurea elastomers synthesized from two different diisocyanates, two different chain extenders and a common aliphatic amine-terminated polyether were used as models to investigate the effects of both diisocyanate structure and aromatic disulfide chain extender on hard segmental packing and self-healing ability. Both direct investigation on hard segments and indirect investigation on chain mobility and soft segmental dynamics were carried out to compare the levels of hard segmental packing, leading to agreed conclusions that correlated well with the self-healing abilities of the polyureas. Both diisocyanate structure and disulfide bonds had significant effects on hard segmental packing and self-healing property. Diisocyanate structure had more pronounced effect than disulfide bonds. Bulky alicyclic isophorone diisocyanate (IPDI) resulted in looser hard segmental packing than linear aliphatic hexamethylene diisocyanate (HDI), whereas a disulfide chain extender also promoted self-healing ability through loosening of hard segmental packing compared to its C-C counterpart. The polyurea synthesized from IPDI and the disulfide chain extender exhibited the best self-healing ability among the four polyureas because it had the highest chain mobility ascribed to the loosest hard segmental packing. Therefore, a combination of bulky alicyclic diisocyanate and disulfide chain extender is recommended for the design of self-healing polyurea elastomers.

2021 ◽  
pp. 095400832110228
Author(s):  
Qiqi Qu ◽  
Hua Wang ◽  
Jing He ◽  
Yunsheng Da ◽  
Menghan Zhu ◽  
...  

The polymers with pH responsiveness and temperature sensitivity exhibit important applications in many fields. To endow the responsive polymers with self-healing is meaningful work, which contributes to increase their service life and reduce waste of resources significantly. In this research, a series of pH-responsive polyurethanes containing dynamic disulfide bonds and carboxylic acid functional groups were prepared by mixing polycaprolactone diol (PCL), hexamethylene diisocyanate (HDI), 2,2-dimethylolbutyric acid, and bis(2-hydroxyethyl) disulfide. The structure of the polymer was confirmed by some characterization methods such as infrared absorption spectroscopy, Raman scattering spectroscopy, X-ray diffraction, and differential scanning calorimetry. Many performances of the polymer such as the contact angle, thermal stability, mechanics, and self-healing properties can be adjusted by changing the functional units of polyurethanes. The dynamic disulfide bonds in the main chain were observed no harm to the pH response performance, instead which were beneficial to the promotion of heat resistance, tensile properties, and self-healing performance of polyurethane. The elongation at break and the tensile strength are increased by 85.3% and 54.9%, respectively. All the polyurethane exhibited considerable self-healing effects at 110°C, with the highest healing efficiency reaching 93.7%, as a result of the dissociation of hydrogen bonds and the exchange reaction of disulfide bonds.


e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Stelian Vlad ◽  
Iuliana Spiridon ◽  
Cristian Vasile Grigoras ◽  
Mioara Drobota ◽  
Alexandra Nistor

AbstractIn this study three series of polyetherurethanes (PEU) based on Terathane ® (polytetramethyleneetherglycol - PTMEG, Mn 1400) as polyol; isophorone diisocyanate (IPDI), 4,4’-methylene-bis-(cyclohexyl-isocyanate) (HMDI) and hexamethylene diisocyanate (HDI) as aliphatic diisocyanate components; 1,4- butanediol (BD) and glycerin (Gly) as chain extenders were synthesized. The glycerin as triol is responsible for the crosslinking structures. All polyether urethanes were synthesized by prepolymer method. The PTMEG was reacted with diisocyanate to realize a diisocyanate-terminated prepolymer, which in next step was extended with blend of the 1,4-butanediol (BD) and glycerin (Gly) in different proportion. The influence of the diisocyanate structure and chain extender functionality on the thermal, mechanical and wettability properties were the aim of this study. The physical, mechanical and wettability properties of these polymers were measured according to standard methods. All polymers were characterized by conventional characterization methods. Different methods of thermal analysis (TGA and DSC) were used for characterization. Wettability was estimated by determination of the dynamic contact angle. The structures were confirmed by FTIR and H-NMR analysis. The results show that the thermal stability, mechanical and wettability properties of the final products are influenced by the diisocyanate and chain extenders nature.


Molecules ◽  
2019 ◽  
Vol 24 (6) ◽  
pp. 1061 ◽  
Author(s):  
Han-Na Kim ◽  
Dae-Woo Lee ◽  
Hoon Ryu ◽  
Gwang-Seok Song ◽  
Dai-Soo Lee

Polyurethane (PU) is a versatile polymer used in a wide range of applications. Recently, imparting PU with self-healing properties has attracted much interest to improve the product durability. The self-healing mechanism conceivably occurs through the existence of dynamic reversible bonds over a specific temperature range. The present study investigates the self-healing properties of 1,4:3,6-dianhydrohexitol-based PUs prepared from a prepolymer of poly(tetra-methylene ether glycol) and 4,4′-methylenebis(phenyl isocyanate) with different chain extenders (isosorbide or isomannide). PU with the conventional chain extender 1,4-butanediol was prepared for comparison. The urethane bonds in 1,4:3,6-dianhydrohexitol-based PUs were thermally reversible (as confirmed by the generation of isocyanate peaks observed by Fourier transform infrared spectroscopy) at mildly elevated temperatures and the PUs showed good mechanical properties. Especially the isosorbide-based polyurethane showed potential self-healing ability under mild heat treatment, as observed in reprocessing tests. It is inferred that isosorbide, bio-based bicyclic diol, can be employed as an efficient chain extender of polyurethane prepolymers to improve self-healing properties of polyurethane elastomers via reversible features of the urethane bonds.


Molecules ◽  
2019 ◽  
Vol 24 (8) ◽  
pp. 1492 ◽  
Author(s):  
Dae-Il Lee ◽  
Seung-Hyun Kim ◽  
Dai-Soo Lee

In this study, environmentally friendly, self-healing waterborne polyurethanes (WPUs) were prepared based on the disulfide metathesis reaction in cystamine. The cystamine acted as a chain extender in the WPU film, which showed a high mechanical strength of 19.1 MPa. The possibility of self-healing reaction was simultaneously modeled via liquid chromatography–mass spectrometry (LC-MS). WPU was confirmed to self-heal a surface crack thermally after a scratch test, and the efficiency was measured by comparing the mechanical properties before and after a cut-and-healing test. In addition, the disulfide-thiol exchange reaction was confirmed to occur in WPU with cystamine as a chain extender and 2-mercaptoethanol. Hot press tests confirmed the possibility of reprocessing the WPU. The WPU incorporating disulfide groups showed great potential as a smart self-healing material.


2021 ◽  
pp. 51371
Author(s):  
Yulong Wang ◽  
Yaqiong Li ◽  
Maoyong He ◽  
Jingjing Bai ◽  
Bingxiao Liu ◽  
...  

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 869
Author(s):  
Minghua Wei ◽  
Shaopeng Wu ◽  
Haiqin Xu ◽  
Hechuan Li ◽  
Chao Yang

Steel slag is the by-product of the steelmaking industry, the negative influences of which prompt more investigation into the recycling methods of steel slag. The purpose of this study is to characterize steel slag filler and study its feasibility of replacing limestone filler in asphalt concrete by evaluating the resistance of asphalt mastic under various aging methods. Firstly, steel slag filler, limestone filler, virgin asphalt, steel slag filler asphalt mastic and limestone filler asphalt mastic were prepared. Subsequently, particle size distribution, surface characterization and pore characterization of the fillers were evaluated. Finally, rheological property, self-healing property and chemical functional groups of the asphalt mastics with various aging methods were tested via dynamic shear rheometer and Fourier transform infrared spectrometer. The results show that there are similar particle size distributions, however, different surface characterization and pore characterization in the fillers. The analysis to asphalt mastics demonstrates how the addition of steel slag filler contributes to the resistance of asphalt mastic under the environment of acid and alkaline but is harmful under UV radiation especially. In addition, the pore structure in steel slag filler should be a potential explanation for the changing resistance of the asphalt mastics. In conclusion, steel slag filler is suggested to replace limestone filler under the environment of acid and alkaline, and environmental factor should be taken into consideration when steel slag filler is applied to replace natural fillers in asphalt mastic.


2021 ◽  
Vol 28 (3) ◽  
Author(s):  
Chenghao Dai ◽  
Xijuan Cao ◽  
Kai Gou ◽  
Qiyan Yin ◽  
Binjie Du ◽  
...  

Author(s):  
Chao Zhou ◽  
Juntao Zhou ◽  
Xiaoqing Ma ◽  
Dicky Pranantyo ◽  
Jingjing Li ◽  
...  

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